[武汉]鼎康（武汉）生物医药有限公司

岗位描述：
?Perform physical-chemical analysis of in-process sample, drug substance, drug product and stability sample according to SOPs.
标准操作规程执行中间控制样品，原液，成品以及稳定性样品的理化分析检测；
?Participate in method transfer, verification and method validation activities which include protocol drafting, execution, data analysis and completing the summary report.
方法转移，确认以及验证的相关活动，包括方案起草，执行，数据分析以及总结报告；
?Create and implement all necessary SOPs.
 必要的标准操作规程的文件；
?Provide daily operation support in QC laboratory, such as equipment maintenance, 5S management.
QC实验室的日常操作支持，例如设备维护，5S管理等；
?Understand technical aspects of the job, best practices, and adhere to cGMP compliance.
工作相关的技术，良好的操作技能，并遵守cGMP合规性；
?Other work arranged by superior leaders.
领导安排的其他工作。